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rs794728055

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728055(A;A)
Make rs794728055(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189007573
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728055
ebirs794728055
HLIrs794728055
Exacrs794728055
Varsomers794728055
Maprs794728055
PheGenIrs794728055
hapmaprs794728055
1000 genomesrs794728055
hgdprs794728055
ensemblrs794728055
gopubmedrs794728055
geneviewrs794728055
scholarrs794728055
googlers794728055
pharmgkbrs794728055
gwascentralrs794728055
openSNPrs794728055
23andMers794728055
23andMe allrs794728055
SNP Nexus

SNPshotrs794728055
SNPdbers794728055
MSV3drs794728055
GWAS Ctlgrs794728055
Max Magnitude0
ClinVar
Risk rs794728055(A;A)
Alt rs794728055(A;A)
Reference rs794728055(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189872299G>A
CLNSRC
CLNACC RCV000181111.1,